My little girl (now 21 months) has Hip Dysplasia (clicky hips for those that think 'huh?' LOL).
I noticed contributing factors at birth (poor abductions and stiffness in leg movement) but also there was positive family history as both myself and my sister had the condition as a child.
Basically docs assured me after birth she was fine. I took her back at 2 weeks old raising my concerns again- fobbed off and told she was fine.
Took her to 6 weeks check after birth- collapsed in tears on a doctor (not my gp a total stranger) saying nobody would listen to me and she examined my daughter and agreed straight away there was a problem.
Time is VITAL in early diagnosis and treatment of this condition as it means the difference between the baby just wearing a Pavlik Harness, or baby having to have surgery and Spica Cast treatment.
So this was November 2004 my daughter was referred to a specialist consultant. Our appointment for ultrasound screening came through 2 months later, and my daughter was eventually seen in February, a whole 3 months later. It was a further month until we saw the consultant again and she was finally treated, but because it had been delayed so much she had to have the surgery and spica cast. It is not fun holding your 5 month old daughter while they give her a general anaesthetic
The treatment lasted 4 months, then she went into a brace for 4 months.
During this time I did HUUUUUUUUUUUUUGE amounts of research on the condition, tried lots of different things and set up a website to help other parents which children with the condition (not sure if allowed to post website address so PM me if anyone wants it).
I found that it is practically protocol throughout the UK to screen babies with family history of the condition as a matter of course, and that my daughter should have received an ultrasound scan on her hips within the first few days of her life.
Contacted a solicitor and the case is ongoing, will take a looooooooong time to sort out and probably cost quite a bit in the long run (good job I have all these bank charges to claim back eh? LOL) but I am determined to ensure that a written procedure is put in place so that no other babies slip through the net. Not even bothered about the money (although we have been told our daughter could end up with a nice amount to be held by the courts and collect when she is 1

I just want them to acknowledge that our daughter suffered unecessarily through a drastic shortfall in her care and poor administration and delays between appointments putting her over the timeline where a Pavlik Harness would have been successful.
Thanks for reading if you got to the end, it was nice to get all that out.
Trace. x
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